Structures of glass-forming liquids by X-ray scattering: Glycerol, xylitol, and D-sorbitol

Author(s):  
Zhenxuan Chen ◽  
Chengbin Huang ◽  
Xin Yao ◽  
Chris J Benmore ◽  
Lian Yu
2009 ◽  
Vol 61 (3) ◽  
pp. 293-295 ◽  
Author(s):  
J.J. Wall ◽  
J.D. Almer ◽  
S.C. Vogel ◽  
P.K. Liaw ◽  
H. Choo ◽  
...  

2000 ◽  
Vol 113 (11) ◽  
pp. 4751-4762 ◽  
Author(s):  
E. Eckstein ◽  
J. Qian ◽  
R. Hentschke ◽  
T. Thurn-Albrecht ◽  
W. Steffen ◽  
...  

2003 ◽  
Vol 18 (10) ◽  
pp. 2494-2500 ◽  
Author(s):  
R. Brüning ◽  
S. Patterson

B2–2xO3–2xH2x glasses were prepared by quenching the melt contained in sealed tubes. The glass-forming range extends from x = 0 to 0.50 (equal to the stoichiometry of metaboric acid, HBO2). The glasses were characterized by differential scanning calorimetry and x-ray scattering. With increasing water content, the glass-transition temperature, Tg, decreases from 553 to 333 K. The specific heat of water-rich samples shows an unusual peak just above Tg. The origin of this peak, which is seen upon heating and cooling, has not been identified. Unlike the composition dependence of Tg, the x-ray structure factors depend for the most part linearly on the composition. In analogy with the crystalline layer compounds α-HBO2 and B(OH)3, the x-ray scattering data show evidence for layering in the medium-range order of water-rich glasses.


2014 ◽  
Vol 783-786 ◽  
pp. 1907-1912
Author(s):  
Shinya Hosokawa

In this article, we show principles and advantages of anomalous x-ray scattering in combination with neutron scattering and reverse Monte Carlo modeling to characterize structures of non-crystalline materials, in particular, metallic glasses. Then, we briefly introduce examples of our recent applications to Pd40Ni40P20and Zr63Ni25Al12bulk metallic glasses having good glass-forming abilities.


2014 ◽  
Vol 140 (14) ◽  
pp. 144906 ◽  
Author(s):  
Toshiji Kanaya ◽  
Rintaro Inoue ◽  
Makina Saito ◽  
Makoto Seto ◽  
Yoshitaka Yoda

Author(s):  
Eva-Maria Mandelkow ◽  
Eckhard Mandelkow ◽  
Joan Bordas

When a solution of microtubule protein is changed from non-polymerising to polymerising conditions (e.g. by temperature jump or mixing with GTP) there is a series of structural transitions preceding microtubule growth. These have been detected by time-resolved X-ray scattering using synchrotron radiation, and they may be classified into pre-nucleation and nucleation events. X-ray patterns are good indicators for the average behavior of the particles in solution, but they are difficult to interpret unless additional information on their structure is available. We therefore studied the assembly process by electron microscopy under conditions approaching those of the X-ray experiment. There are two difficulties in the EM approach: One is that the particles important for assembly are usually small and not very regular and therefore tend to be overlooked. Secondly EM specimens require low concentrations which favor disassembly of the particles one wants to observe since there is a dynamic equilibrium between polymers and subunits.


Author(s):  
Eva-Maria Mandelkow ◽  
Ron Milligan

Microtubules form part of the cytoskeleton of eukaryotic cells. They are hollow libers of about 25 nm diameter made up of 13 protofilaments, each of which consists of a chain of heterodimers of α-and β-tubulin. Microtubules can be assembled in vitro at 37°C in the presence of GTP which is hydrolyzed during the reaction, and they are disassembled at 4°C. In contrast to most other polymers microtubules show the behavior of “dynamic instability”, i.e. they can switch between phases of growth and phases of shrinkage, even at an overall steady state [1]. In certain conditions an entire solution can be synchronized, leading to autonomous oscillations in the degree of assembly which can be observed by X-ray scattering (Fig. 1), light scattering, or electron microscopy [2-5]. In addition such solutions are capable of generating spontaneous spatial patterns [6].In an earlier study we have analyzed the structure of microtubules and their cold-induced disassembly by cryo-EM [7]. One result was that disassembly takes place by loss of protofilament fragments (tubulin oligomers) which fray apart at the microtubule ends. We also looked at microtubule oscillations by time-resolved X-ray scattering and proposed a reaction scheme [4] which involves a cyclic interconversion of tubulin, microtubules, and oligomers (Fig. 2). The present study was undertaken to answer two questions: (a) What is the nature of the oscillations as seen by time-resolved cryo-EM? (b) Do microtubules disassemble by fraying protofilament fragments during oscillations at 37°C?


1992 ◽  
Vol 2 (6) ◽  
pp. 899-913 ◽  
Author(s):  
Patrick Davidson ◽  
Elisabeth Dubois-Violette ◽  
Anne-Marie Levelut ◽  
Brigitte Pansu

1996 ◽  
Vol 6 (8) ◽  
pp. 1085-1094 ◽  
Author(s):  
A. Gibaud ◽  
J. Wang ◽  
M. Tolan ◽  
G. Vignaud ◽  
S. K. Sinha

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